104876-54-2Relevant articles and documents
Stereodivergent synthesis of pseudotabersonine alkaloids
Kazak, Mihail,Priede, Martins,Shubin, Kirill,Bartrum, Hannah E.,Poisson, Jean-Fran?ois,Suna, Edgars
, p. 5356 - 5359 (2017)
An eight-step stereodivergent synthesis of enantiomerically pure (-)-14-epi-pseudotabersonine and (+)-pseudotabersonine has been developed from a common N-tert-butanesulfinyl ketimine key intermediate.
Indoles and Indole Alkaloids, XXI. - Preparation of 4-(Acetylamino)-1,2,3,9a-tetrahydrocarbazole Derivatives by Cycloadditions of 3-Indolyl-enimides and -enamides
Goetz, Peter Heinz,Bats, Jan Willem,Fritz, Helmut
, p. 2065 - 2080 (2007/10/02)
Treatment of the oximes of the 3-acetylindoles 1 and 5 with acetic anhydride in pyridine results in the formation of the enimides 2 and 7, which slowly undergo cycloadditions with acrolein and derivatives of acrylic acid to form 3 and 10, respectively.Com